Evidence map›Paper›PMID 39906432›Full record

ArticleCureus2025

Clinical Outcomes and Healthcare Utilization in Pulmonary Embolism Patients With and Without Prothrombin G20210A Mutation: A National Retrospective Cohort Study.

Fahmida Sultana, Ribaba Rayan, Tasnim Jabbar Brishti, Iffath Mizan, Sabrina Sifat, Fnu Ifatujjahan, Juan Carlos Sequeira Gross, Garry Aliosha Francis Morel

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Article in Cureus, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

8 authors.

Fahmida SultanaMedicine, Washington University of Health and Sciences, San Pedro, BLZ.
Ribaba RayanInternal Medicine, Shaheed Suhrawardy Medical College and Hospital, Dhaka, BGD.
Tasnim Jabbar BrishtiMedicine, Ibrahim Medical College, Dhaka, BGD.
Iffath MizanMedicine, El Camino Hospital, Mountain View, USA.
Sabrina SifatMedicine, Kumudini Women's Medical College, Tangail, BGD.
Fnu IfatujjahanMedicine, Shaheed Ziaur Rahman Medical College, Bogra, BGD.
Juan Carlos Sequeira GrossInternal Medicine, Lee Memorial Health System, Gulf Coast Medical Center, Fort Myers, USA.
Garry Aliosha Francis MorelDepartment of Medicine, Division of Pulmonary, Critical Care and Sleep Medicine, Saint Louis University Hospital, St. Louis, USA.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPulmonary embolism (PE) is a severe condition often linked to thromboembolic risk factors, such as the prothrombin gene (PGM) G20210A mutation. Although this mutation is a recognized risk factor for venous thromboembolism, little is known about how it affects the clinical course and healthcare utilization of PE patients.

objectiveThis new study will reveal the complete effect of PGM on clinical outcomes in patients treated for PE, such as hospital stay length, in-hospital death rates, healthcare costs, and associated health conditions. It will also examine how socioeconomic status and demographics impact these outcomes.

methodsThis retrospective cohort study was conducted using data from the National Inpatient Sample (NIS) from 2016 to 2020. It included adults admitted with a primary diagnosis of PE aged 18 and older. The patients were divided into two groups: those with the PGM mutation and those without. There were two groups where the patients was divided based on their PGM use: those with and those without. Multivariate logistic regression assessed in-hospital mortality, while linear regression models evaluated length of stay (LOS) and healthcare charges. The models were adjusted for demographics, comorbidities (Charlson Comorbidity Index), and hospital characteristics.

resultsAmong the 903,230 PE patients, 2,065 (0.2%) had PGM. Patients with the mutation had a significantly lower in-hospital mortality than those without the mutation (adjusted OR 0.13, 95% CI 0.02-0.92, p = 0.041). PGM carriers also had lower rates of atrial fibrillation (5.1% vs. 11.8%, p < 0.001), congestive heart failure (CHF) (5.9% vs. 16.0%, p < 0.001), and chronic obstructive pulmonary disease (COPD) (8.6% vs. 15.5%, p < 0.001), but higher rates of obesity (32.5% vs. 26.1%, p = 0.004) and hyperlipidemia (30.7% vs. 36.0%, p = 0.031). Despite a longer hospital stay in PGM patients (mean difference: 0.52 days, p = 0.005), the difference in total hospital charges was not statistically significant (mean difference: $6,295, p = 0.090).

conclusionsPatients with PE and the PGM had lower mortality rates in this national retrospective cohort than those without the mutation. Patients without the PGM presented with more serious comorbidities, including higher rates of atrial fibrillation, CHF, and COPD, which may have contributed to their worse outcomes.

Indexed as

comorbiditiesg20210amortalitynational inpatient sampleprothrombin gene mutationpulmonary embolism

Identifiers

PMID39906432
PMCPMC11790415

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